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首页> 外文期刊>Life sciences >Varenicline and nicotine enhance GABAergic synaptic transmission in rat CA1 hippocampal and medial septum/diagonal band neurons
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Varenicline and nicotine enhance GABAergic synaptic transmission in rat CA1 hippocampal and medial septum/diagonal band neurons

机译:缬氨酸和尼古丁增强大鼠CA1海马和内侧中隔/对角带神经元的GABA能突触传递

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摘要

Aims The FDA approved smoking cessation aid varenicline can effectively attenuate nicotine-stimulated dopamine release. Varenicline may also exert important actions on other transmitter systems that also influence nicotine reinforcement or contribute to the drug's cognitive and affective side effects. In this study, we determined if varenicline, like nicotine, can stimulate presynaptic GABA release. Main methods Using whole-cell patch-clamp techniques, we measured GABAAR-mediated asynchronous, spontaneous miniature inhibitory postsynaptic currents (mIPSCs) in acute brain slices from two brain regions important for learning and memory, the hippocampus and basal forebrain. Key findings Both varenicline (10 ??M) and nicotine (10 ??M) applications alone resulted in small but significant increases in amplitude, as well as robustly enhanced frequency of mIPSCs in hippocampal CA1 pyramidal neurons and medial septum/diagonal band (MS/DB) neurons. A unique subpopulation of MS/DB neurons showed decreases in frequency. In the presence of nicotine, varenicline effectively attenuated the expected enhancement of hippocampal mIPSC frequency like a competitive antagonist. However, in the MS/DB, varenicline only partially attenuated nicotine's effects. Reversing the order of drug application by adding nicotine to varenicline-exposed slices had little effect. Significance Varenicline, like nicotine, stimulates presynaptic GABA release, and also exerts a partial agonist action by attenuating nicotine-stimulated release in both the hippocampus and basal forebrain. These effects could potentially affect cognitive functions. ? 2013 Elsevier Inc. All rights reserved.
机译:目的FDA批准的戒烟辅助药缬尼克兰可有效减轻尼古丁刺激的多巴胺释放。瓦伦尼克林还可能在其他递质系统上发挥重要作用,这些系统也会影响尼古丁的强化或促进药物的认知和情感副作用。在这项研究中,我们确定了伐尼克兰是否像尼古丁一样可以刺激突触前GABA的释放。主要方法使用全细胞膜片钳技术,我们在两个对学习和记忆至关重要的大脑区域(海马和基底前脑)的急性脑切片中测量了GABAAR介导的异步,自发微型抑制性突触后突触电流(mIPSC)。主要发现伐尼克兰(10 ?? M)和尼古丁(10 ?? M)的单独应用都会导致海马CA1锥体神经元和内侧中隔/对角带(MS / DB)神经元。 MS / DB神经元的唯一亚群显示频率降低。在存在尼古丁的情况下,伐尼克兰像竞争性拮抗剂一样有效地减弱了海马mIPSC频率的预期增强。但是,在MS / DB中,缬尼克兰仅能部分减弱尼古丁的作用。通过将尼古丁添加到暴露于伐尼克兰的片中来改变药物施用的顺序几乎没有效果。重要性瓦伦尼克碱与尼古丁一样,可刺激突触前GABA的释放,并通过减弱海马和基底前脑中尼古丁刺激的释放来发挥部分激动剂作用。这些影响可能会影响认知功能。 ? 2013 Elsevier Inc.保留所有权利。

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